chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143897818143897819AG15GENIChomozygous126541605
7143898110143898111CT14GENIChomozygous126541606
7143898390143898391CA8GENIChomozygous126541607
7143898896143898897TA12GENIChomozygous126541608
7143899130143899131TG21GENIChomozygous126541609
7143899442143899443GA19GENIChomozygous126541610
7143899540143899541AG23GENIChomozygous126541611
7143900309143900310GT8GENIChomozygous126541612
7143900594143900595TC21GENIChomozygous126541613
7143901849143901850GA9GENIChomozygous126541614
7143902109143902110GA8GENIChomozygous126541615
7143902164143902165CT5GENIChomozygous126541616
7143902243143902244CA25GENIChomozygous126541617
7143902779143902780AG14GENIChomozygous126541618
7143903239143903240CT20GENIChomozygous126541619
7143903507143903508GA8GENICheterozygous126541620
7143903538143903539CA3GENICheterozygous126541621
7143904947143904948AC22GENICheterozygous126541622
7143905062143905063AG21GENIChomozygous126541623
7143905889143905890AG16GENIChomozygous126541624
7143906758143906759AG22GENIChomozygous126541625
7143907072143907073CT20GENIChomozygous126541626
7143908207143908208CT9GENIChomozygous126541627
7143908992143908993CT23GENIChomozygous126541628
7143909021143909022GA22GENIChomozygous126541629
7143909402143909403TC23GENIChomozygous115944782
7143909478143909479TC22GENIChomozygous115944783
7143911536143911537CA12GENIChomozygous115944784
7143913006143913007AG30GENIChomozygous115944785
7143913815143913816AG21GENIChomozygous115944786